Canonical Allele Identifier: CA2484369518
Gene: IRF6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.209801183_209801195delinsCAAAAAAAAAAAA , CM000663.2:g.209801183_209801195delinsCAAAAAAAAAAAA GRCh38
NC_000001.10:g.209974528_209974540delinsCAAAAAAAAAAAA , CM000663.1:g.209974528_209974540delinsCAAAAAAAAAAAA GRCh37
NC_000001.9:g.208041151_208041163delinsCAAAAAAAAAAAA NCBI36
NG_007081.2:g.9940_9952delinsTTTTTTTTTTTTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000696133.1:c.174+45_174+57delinsTTTTTTTTTTTTG ENSP00000512426.1:n.174+45_174+57delinsTTTTTTTTTTTTG
ENST00000696134.1:c.174+45_174+57delinsTTTTTTTTTTTTG ENSP00000512427.1:n.174+45_174+57delinsTTTTTTTTTTTTG
ENST00000367021.8:c.174+45_174+57delinsTTTTTTTTTTTTG MANE Select ENSP00000355988.3:n.174+45_174+57delinsTTTTTTTTTTTTG
ENST00000643798.1:c.174+45_174+57delinsTTTTTTTTTTTTG ENSP00000496669.1:n.174+45_174+57delinsTTTTTTTTTTTTG
ENST00000367021.7:c.174+45_174+57delinsTTTTTTTTTTTTG ENSP00000355988.3:n.174+45_174+57delinsTTTTTTTTTTTTG
ENST00000456314.1:c.174+45_174+57delinsTTTTTTTTTTTTG ENSP00000403855.1:n.174+45_174+57delinsTTTTTTTTTTTTG
ENST00000542854.5:c.-111-4643_-111-4631delinsTTTTTTTTTTTTG ENSP00000440532.1:n.-111-4643_-111-4631delinsTTTTTTTTTTTTG
NM_001206696.1:c.-111-4643_-111-4631delinsTTTTTTTTTTTTG NP_001193625.1:n.-111-4643_-111-4631delinsTTTTTTTTTTTTG
NM_006147.3:c.174+45_174+57delinsTTTTTTTTTTTTG NP_006138.1:n.174+45_174+57delinsTTTTTTTTTTTTG
NM_006147.4:c.174+45_174+57delinsTTTTTTTTTTTTG MANE Select NP_006138.1:n.174+45_174+57delinsTTTTTTTTTTTTG
NM_001206696.2:c.-111-4643_-111-4631delinsTTTTTTTTTTTTG NP_001193625.1:n.-111-4643_-111-4631delinsTTTTTTTTTTTTG